Canonical Allele Identifier: CA5921078
Community Standard Title: NM_004211.5(SLC6A5):c.419C>A (p.Thr140Asn)
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20601544C>A , CM000673.2:g.20601544C>A GRCh38
NC_000011.9:g.20623090C>A , CM000673.1:g.20623090C>A GRCh37
NC_000011.8:g.20579666C>A NCBI36
NG_013086.1:g.7145C>A
NG_013086.2:g.7145C>A

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.419C>A MANE Select NP_004202.4:p.Thr140Asn
ENST00000525748.6:c.419C>A MANE Select ENSP00000434364.2:p.Thr140Asn
NM_001318369.1:c.-145C>A NP_001305298.1:n.-145C>A
NM_001318369.2:c.-145C>A NP_001305298.1:n.-145C>A
NM_004211.3:c.419C>A NP_004202.2:p.Thr140Asn
NM_004211.4:c.419C>A NP_004202.3:p.Thr140Asn
ENST00000298923.11:c.419C>A ENSP00000298923.7:p.Thr140Asn
ENST00000525748.5:c.419C>A ENSP00000434364.1:p.Thr140Asn
XM_005253225.1:c.-145C>A XP_005253282.1:n.-145C>A
XM_011520473.1:c.419C>A XP_011518775.1:p.Thr140Asn
XM_017018545.2:c.-57+1869C>A XP_016874034.1:n.-57+1869C>A